Noack syndrome

Noack syndrome
Pfeiffer s.

Medical dictionary. 2011.

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  • Noack syndrome — No·ack syndrome (noґahk) [Margot Noack, German physician, 20th century] Pfeiffer syndrome; see under syndrome …   Medical dictionary

  • Syndrome de pfeiffer — Le syndrome de Pfeiffer est une craniosynostose en rapport avec une mutation du gène FGPR. Cette mutation du gène FGPR est responsable d autres craniosynostose regroupées sous le nom de craniosynostose FGPR dépendante. Les sutures du crâne qui… …   Wikipédia en Français

  • Syndrome de Pfeiffer — Le syndrome de Pfeiffer est une craniosynostose en rapport avec une mutation du gène FGPR. Cette mutation du gène FGPR est responsable d autres craniosynostose regroupées sous le nom de craniosynostose FGPR dépendante. Les sutures du crâne qui… …   Wikipédia en Français

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Noack — M., 20th century German physician. See N. syndrome …   Medical dictionary

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  • Pfeiffer syndrome — A form of craniosynostosis that results in multiple physical defects, including broad thumbs and great toes; depressed nasal bridge and generally flat profile; low set, slanted ears;, strabismus; and a prominent mandible. There may also be… …   Medical dictionary

  • Acrocephalosyndactylia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD10|Q|87|0|q|80 ICD9 = ICD9|755.55 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D000168 Acrocephalosyndactylia (or acrocephalosyndactyly) is the common… …   Wikipedia

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  • Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 …   Wikipedia

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